An overview of Middle East respiratory syndrome coronavirus vaccines in preclinical studies

被引:13
作者
Zhang, Naru [1 ]
Shang, Jian [2 ]
Li, Chaoqun [1 ]
Zhou, Kehui [1 ]
Du, Lanying [3 ]
机构
[1] Zhejiang Univ City Coll, Sch Med, Dept Clin Med, Hangzhou, Peoples R China
[2] Univ Minnesota, Coll Vet Med, Dept Vet & Biomed Sci, St Paul, MN 55108 USA
[3] New York Blood Ctr, Lindsley F Kimball Res Inst, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
Coronavirus; MERS-CoV; spike protein; structural proteins; non-structural proteins; vaccines; preclinical studies; RECEPTOR-BINDING DOMAIN; DIPEPTIDYL PEPTIDASE 4; CELLULAR IMMUNE-RESPONSES; N-TERMINAL DOMAIN; MERS-COV; SPIKE PROTEIN; NEUTRALIZING ANTIBODIES; SAUDI-ARABIA; MOUSE MODEL; FUNCTIONAL RECEPTOR;
D O I
10.1080/14760584.2020.1813574
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction Middle East respiratory syndrome coronavirus (MERS-CoV) causes high mortality in humans. No vaccines are approved for use in humans; therefore, a consistent effort to develop safe and effective MERS vaccines is needed. Areas covered This review describes the structure of MERS-CoV and the function of its proteins, summarizes MERS vaccine candidates under preclinical study (based on spike and non-spike structural proteins, inactivated virus, and live-attenuated virus), and highlights potential problems that could prevent these vaccines entering clinical trials. It provides guidance for the development of safe and effective MERS-CoV vaccines. Expert opinion Although many MERS-CoV vaccines have been developed, most remain at the preclinical stage. Some vaccines demonstrate immunogenicity and efficacy in animal models, while others have potential adverse effects or low efficacy against high-dose or divergent virus strains. Novel strategies are needed to design safe and effective MERS vaccines to induce broad-spectrum immune responses and improve protective efficacy against multiple strains of MERS-CoV and MERS-like coronaviruses with pandemic potential. More funds should be invested to move vaccine candidates into human clinical trials.
引用
收藏
页码:817 / 829
页数:13
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